Mode
Text Size
Log in / Sign up
N/A N=79 Other

Improving Cesarean Section Experience Through Hypnotherapy

Cesarean Section · Pain · Anxiety

Enrolled (actual)
79
Serious AEs
0.0%
Results posted
Mar 2017
Primary outcome: Primary: Wellbeing Measured Using a Comfort Scale — 6.7; 8.0 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
hypnosis (Other)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Groupe Hospitalier de la Rochelle Ré Aunis
Primary completion
Oct 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Wellbeing Measured Using a Comfort Scale
8.9; 8.8
SECONDARY
Wellbeing Measured Using a Comfort Scale
8.9; 8.8
SECONDARY
Wellbeing Measured Using a Comfort Scale
8.9; 8.8
SECONDARY
Score at Numeric Pain Rating Scale
1.1; 1.1
SECONDARY
Score at Numeric Pain Rating Scale
1.1; 1.1
SECONDARY
Score at Numeric Pain Rating Scale
1.1; 1.1
SECONDARY
Mean Blood Pressure
87; 88
SECONDARY
Mean Blood Pressure
87; 88
SECONDARY
Mean Blood Pressure
87; 88
SECONDARY
Mean Pulse
86; 84
SECONDARY
Mean Pulse
86; 84
SECONDARY
Mean Pulse
86; 84
SECONDARY
Non-steroidal Anti-inflammatory Drug Intake
43; 18

Summary

Cesarean section rates continue to increase worldwide, particularly in middle- and high-income countries. In France, the rate has now stabilized around 20 %. Cesarean section is a particular way of giving birth, sometimes desired, but sometimes feared. If some women do not feel affected by this way of giving birth, it is more difficult for others to live with. In this way, not being able to give birth trough natural way may be disturbing in motherhood. At La Rochelle hospital, more than 230 healthcare providers have been trained according to Erickson's hypnosis methodology. Among them, 40 are part of the anesthesia department and a committee oversees the hypnotherapist activities in pain management. The objective of the present study is to assess the benefit of hypnosis session for improving experience and reducing anxiety in women giving birth through surgery.

Eligibility Criteria

Inclusion Criteria

  • over 18
  • scheduled or unplanned cesarean section
  • Informed consent

Exclusion Criteria

  • Refusal of the patient to participate in the study
  • Not French speaking
  • Patients under guardianship
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02418026). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search